Effect of lifestyle intervention in patients with type 2 diabetes: A meta ...

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Metabolism www.metabolismjournal.com

Effect of lifestyle intervention in patients with type 2 diabetes: A meta-analysis Liang Chen⁎, Jian-Hao Pei, Jian Kuang, Hong-Mei Chen, Zhong Chen, Zhong-Wen Li, Hua-Zhang Yang The First Division in Department of Endocrinology, Guangdong General Hospital, Guangdong Academy of Medical Sciences, 106th of Zhongshan Er Road, Guangzhou 510080, China

A R T I C LE I N FO Article history:

AB S T R A C T Objective. The effect of lifestyle intervention on clinical risk factors in patients with type

Received 16 June 2014

2 diabetes is unclear. The aim of this meta-analysis was to evaluate the effects of

Accepted 19 October 2014

comprehensive lifestyle change, such as diet, exercise, and education, on clinical markers that are risk-factors for cardiovascular disease in patients with type 2 diabetes.

Keywords:

Methods. We searched Medline, Cochrane, EMBASE, and Google Scholar (up to August 31,

Lifestyle

2013) for randomized controlled trials that compared standard of care (control group) with

Intervention

treatment regimens that included changes in lifestyle (intervention group). The primary

Type 2 diabetes

outcome was reduction in risk factors of cardiovascular disease including body mass index

Meta-analysis

(BMI), glycated hemoglobin (HbA1c), systolic blood pressure (SBP), diastolic blood pressure (DBP), high-density lipoprotein cholesterol (HDL-c), and low-density lipoprotein cholesterol (LDL-c). Results. A total of 16 studies were included in the meta-analysis. The standardized difference in means of change from baseline significantly favored the intervention compared with the control group in BMI (−0.29; 95% CI, −0.52 to −0.06, P = 0.014), HbA1c (−0.37; 95% CI, −0.59 to −0.14, P = 0.001), SBP (−0.16: 95% CI, −0.29 to −0.03, P = 0.016), DBP (−0.27, 95% CI = −0.41 to −0.12, P < 0.001). There was no difference between the intervention and control groups in HDL-c (0.05; 95% CI, −0.10 to 0.21; P = 0.503) and LDL-c (−0.14; 95% CI, −0.29 to 0.02; P = 0.092). Conclusions. The meta-analysis found that lifestyle intervention showed significant benefit in risk factors that are known to be associated with development of cardiovascular disease in patients with type 2 diabetes. © 2015 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NCND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).

1.

Introduction

The proportion of people with type 2 diabetes is on the rise and is a major cause of death world-wide. Type 2 diabetes is a major risk factor for vascular disease with 65% of all diabetic deaths being due to cardiovascular disease [1]. Lifestyle characteristics, such as physical activity, diet, and stress are important factors that influence development and

prognosis of type 2 diabetes [2]. Changes in diet and increase in physical activity (walking, etc.) and exercise (running, cycling, etc.) are key components of the management of type 2 diabetes [3], and guidelines recommend changes in these lifestyle characteristics for both prevention and management of the disease [4]. Several systematic reviews and meta-analyses have reported the benefit of interventions aimed at improving lifestyle

Abbreviations: BMI, body mass index; HbA1c, glycated hemoglobin; SBP, systolic blood pressure; DBP, diastolic blood pressure; HDL-c, high-density lipoprotein cholesterol; LDL-c, low-density lipoprotein cholesterol. ⁎ Corresponding author. Tel.: +86 13538785491. E-mail address: [email protected] (L. Chen). http://dx.doi.org/10.1016/j.metabol.2014.10.018 0026-0495/© 2015 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons. org/licenses/by-nc-nd/3.0/).

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behaviors on disease progression and development of comorbidities (eg, vascular disease) in patients with type 2 diabetes [5–13]. However, the benefit of lifestyle changes in reducing all-cause mortality or cardiovascular disease is less clear as the findings from these analyses are inconsistent or the data are inconclusive [5–13]. To our knowledge, there have been no meta-analyses that evaluated the effect of interventions that result in multiple lifestyle changes on risk factors for cardiovascular disease in patients with type 2 diabetes. The aim of this meta-analysis was to evaluate the effects of changes in lifestyle that included dietary behavior, exercise, or physical activities on clinical markers of cardiovascular disease in patients with type 2 diabetes.

2.

Materials and methods

2.1.

Search strategy

We searched Medline, Cochrane, EMBASE, and Google Scholar for randomized controlled trials that compared standard care with interventions that involved changes in lifestyle. The following terms were used in the search: diabetes, cardiovascular risk, lifestyle, health education, dietary, exercise/physical activities, and behavioral intervention. Articles up to August 31, 2013 were included. Studies were excluded if they were not published in English, were not prospective randomized trials, did not enroll patients with type 2 diabetes, or did not investigate lifestyle or education programs relating to dietary behavior, exercise, or physical activities. All possibly relevant studies were also hand-searched by 2 independent reviewers and both reviewers had to agree for the study to be included. If there was disagreement, it was resolved by a third reviewer.

2.2.

Data extraction

The following information or data were extracted from the included studies: the name of the first author, year of publication, study design, number of participants in each treatment group, participants' age and gender, diagnostic criteria, intervention regiment for study/control group, and results.

2.3.

Quality assessment

The included studies were assessed for risk bias using the ‘Risk of Bias’ assessment tool, Review Manager 5.1, and recommendations for judging risk of bias provided in Chapter 8 of the Cochrane Handbook for Systematic Reviews Interventions [14].

2.4.

339

the percentage of the total variability in effect estimates among trials resulting from heterogeneity rather than chance. Random-effects models of analysis were used if heterogeneity was detected (I2 > 50%). Otherwise, fixed-effects models were used. For each risk factor measure, standardized difference in means with corresponding 95% confidence intervals (CIs) was calculated for between groups and among studies. A twosided P value < 0.05 indicated statistical significance for one comparison group over the other. Sensitivity analysis was carried out for the risk factors BMI and HbA1c using the leave one-out approach. A funnel plot, the fail-safe N (which indicates whether the observed significance is spurious or not), and Egger's test (which detects whether the observed studies is asymmetric or not) were used to assess possible publication bias. All analyses were performed using Comprehensive Meta-Analysis statistical software, version 2.0 (Biostat, Englewood, NJ).

3.

Results

3.1.

Characteristics of included studies

Eighty-five possible studies were identified and 18 were excluded owing to not being relevant to this analysis (Fig. 1). Of the 67 remaining studies, 51 were excluded due to being redundant with an included study, not presenting outcomes of interest, having an intervention period of 2 treatment arms. One study [15] met the inclusion criteria but was excluded because its findings, in regard to BMI, LDL-c and HDL-c changes, were not in concordance with the included studies. The inclusion of this study would have skewed the meta-analysis by increasing the discrepancy in both sensitivity and publication bias analyses (Fig. 1). A total of 16 studies were included in the meta-analysis [16–31]. The number of patients per study ranged from 23 to 2575 (Table 1). The mean (SD) age was similar across studies (range, 51.3 [1.8] to 67.3 [19]) and between the interventional and control groups (Table 1). The proportion of patients that were male ranged from 34.8% to 98%, and the lengths of the study ranged from 6 months to 8 years (Table 1). Supplementary Table S1 summarizes the change from baseline of key risk factors for all included studies. Quality assessment indicated that all 16 studies had a high risk of performance bias due to the studies not having adequate blinding of the participants and personnel (Fig. 2A and B). Six studies had high risk of bias due to risk factor assessments not being blinded (Fig. 2B) [16,22–24,30,31].

Statistical analysis 3.2.

The primary outcome was reduction in any risk factor of cardiovascular disease including body mass index (BMI), HbA1c, systolic blood pressure (SBP), diastolic blood pressure (DBP), high-density lipoprotein-c (HDL-c), and low-density lipoprotein-c (LDL-c). BMI, HbA1c, SBP, DBP, HDL-c, and LDL-c were compared between participants having intensive lifestyle intervention (intervention group) and conventional intervention (control group). A χ2 based test of homogeneity was performed using Cochran's Q statistic and I2. I2 illustrates

Body mass index

Eleven of the included studies reported change from baseline in BMI [18–20,22–25,27,28,30,31]. There was heterogeneity for BMI across studies (Q statistic = 71.93, I 2 = 86.10%, P < 0.001); hence, a random effects analysis was applied. The standardized difference in means of change from baseline in BMI significantly favored the intervention group over the control group (standardized difference in means, − 0.29; 95% CI, − 0.52 to − 0.06, P = 0.014) (Fig. 3).

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Fig. 1 – Flow chart for study selection.

3.3.

HbA1c

All 16 studies reported data for change from baseline in HbA1c. A random effects analysis was applied owing to evidence of heterogeneity among the studies (Q statistic = 238.84, I2 = 93.72%, P < 0.001). The standardized difference in means of change from baseline in HbA1c significantly favored the intervention group compared with the control group (standardized difference in means, − 0.37; 95% CI, − 0.59 to − 0.14, P = 0.001) (Fig. 3).

3.4.

Systolic and diastolic blood pressure

Fifteen of the 16 studies reported values for SBP at baseline and following intervention [16–28,30,31] and 14 reported DBP [16–25,27,28,30,31]. There was heterogeneity across the studies in both SBP and DBP (SBP: Q statistic = 64.03, I2 = 78.13%, P < 0.001; DBP: Q statistic = 73.51, I 2 = 82.32%, P < 0.001); consequently, a random effects analysis was used. The standardized difference in means of change from baseline in both SBP and DBP significantly favored the intervention (SBP: standardized difference in means, − 0.16: 95% CI, − 0.29 to − 0.03, P = 0.016; DBP: standardized difference in means: − 0.27, 95% CI = −0.41 to − 0.12, P < 0.001) (Fig. 3).

was applied for both risk factors as there was evidence of heterogeneity among the studies (LDL-c: Q statistic = 48.77, I2 = 77.45%, P < 0.001; HDL-c: Q statistic = 72.93, I2 = 83.55%, P < 0.001). The standardized difference in mean change from baseline showed no difference between groups for both HDL-c and LDL-c (HDL-c: standardized difference in means, 0.05; 95% CI, − 0.10 to 0.21; P = 0.503; LDL-c: standardized difference in means = − 0.14; 95% CI, −0.29 to 0.02; P = 0.092) (Fig. 3).

3.6.

Sensitivity analysis was performed in which the results were analyzed when one study was removed in turn for BMI and HbA1c results. The direction and magnitude of the combined estimates did not markedly change with the exclusion of individual studies, indicating that no one study dominated the findings (Fig. 4). Funnel plot analysis for publication bias found the combined effect size yielded Z values of 1.96 for BMI (P < 0.001) and − 8.16 for HbA1c (P < 0.001). The Eggar's test found funnel plot symmetry, indicating there was no significant evidence of publication bias (P = 0.148 for BMI, P = 0.572 for HbA1c) (Fig. 5).

4. 3.5.

Sensitivity analysis and publication bias

Discussion

LDL-c and HDL-c

Of the 16 studies, 12 reported change from baseline in LDL-c [16,17,20–23,25,26,28–31] and 13 reported change from baseline in HDL-c [16–20,22–25,28–31]. A random effects analysis

The effect of lifestyle interventions on risk factors associated with cardiovascular disease in patients with type 2 diabetes is unclear. Only a limited number of studies have investigated this issue and they utilized a range of interventions and

Table 1 – Baseline characteristics of studies included in the meta-analysis. Type of study

Total enrolled patient number

Groups

Description of groups

Number of patients

Age, y (mean ± SD)

Sex, males (n, %)

Length of program

Ali M (2012)

RCT

48

Intervention

Pharmaceutical care package (education program of about diabetes, its treatment and associated cardiovascular risk factors) Seen by a pharmacist only at the beginning of the study and then after 12 months in addition to the usual service. Pharmacist care Without pharmacist interventions Supervised exercise General advice about physical activity Group counseling sessions over the diabetes selfmanagement regimen Monthly contact with the study team Education Medication Optimization group (a structured selfmanagement education program) Standard care by their own clinician according to local guidelines Precede Health Promotion Education (PHPE) Conventional Health Promotion Education (CHPE) Intensive lifestyle intervention (ILI) Diabetes support and education (DSE) Dietary intensive individualized dietary intervention Usual clinical care for diabetes Lifestyle intervention (education on lifestyle modification) Conventional treatment Regular, structured and personalized exercise prescription Usual outpatient clinical care Supervised training plus structured exercise counseling Counseling alone as part of standard care Additional structured health education program Usual medical care only Supervised by a signed case manager Usual care from the primary care provider Physical activity counseling intervention Standard exercise leaflet Systemic education program in group and individual sessions Usual care Intensified diet education Usual care at local health centers

23

66.4 ± 12.7

10, 43.5%

12 months

23

66.8 ± 10.2

13, 56.5%

51 54 70 70 132

63.2 ± 9.5 61.7 ± 11.2 57 ± 6 56 ± 6 NA

30, 58.8% 28, 51.9% 41, 59% 40, 57% 38, 29%

6 months

133 94

NA 62.6 ± 10.3

46, 34.8% 71, 75.5%

18 months

95 300 300 2570 2575 45 48 1017 1016 32 29 303 303 90 88 123 123 35 35 56 56 40 46

60.3 ± 10.7 66.06 ± 8 67.28 ± 19 58.6 ± 6.8 58.9 ± 6.9 56.6 ± 8.8 58.4 ± 8.8 58.5 ± 6.9 58.6 ± 7.0 54.3 ± 1.4 51.3 ± 1.8 NA NA 55.0 ± 9.0 56.0 ± 10.2 61 ± 10 61 ± 11 57.6 ± 7.9 NA 62.0 (35–80) ⁎ 61.0 (43–78) ⁎ NA NA

72, 75.8% 139, 46.2% 152, 50.7% 1044, 40.7% 1038, 40.4% 17,38% 21, 44% 549, 54.0% 538, 53.0% 20,62% 18, 62% NA NA 44, 48.9% 34, 38.6% 121, 98% 117, 95% 35, 50% NA 27, 48.2% 34, 60.7% NA NA

Control Chan CW (2012)

RCT

120

Dobrosielski DA (2012)

RCT

140

Sevick MA (2012)

RCT

265

Intervention Control Intervention Control Intervention

Crasto W (2011)

RCT

189

Control Intervention

Salinero-Fort MA (2011)

RCT

608

The LookAHEAD Research Group (2010) Coppell KJ (2010)

RCT

5145

RCT

93

Sone H (2010)

RCT

2033

Wisse W (2010)

RCT

74

Balducci S (2010)

RCT

606

Ko GT (2004)

RCT

180

Krein SL (2004)

RCT

246

Kirk A (2004)

RCT

70

Trento M (2002)

RCT

112

Uusitupa M (1993)

RCT

86

Control Intervention Control Intervention Control Intervention Control Intervention Control Intervention Control Intervention Control Intervention Control Intervention Control Intervention Control Intervention Control Intervention Control

9 months 26 weeks

2 years 4 years 6 months 8 years 2 years 12 months 1 year 18 months 12 months

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Study

4 years 15 months

Abbreviations: NA, not available; RCT, randomized control trial. ⁎ Median (range: min. to max.).

341

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Fig. 2 – The quality assessment for each included study was summarized in (A) risk of bias summary or (B) as percentages across all included studies in risk of bias graph.

methodologies [16–31]. Interventions included increased physical activity, reduced caloric intake, dietary education, and counseling and education regarding treatment adherence or disease monitoring. In general, these studies indicated a benefit of lifestyle intervention on risk factors of cardiovascular disease [16–31]. However, not all findings were consistent across studies. For example, Dobrosieski et al. (2012) found no change in blood pressure with supervised exercise [27] while, Balducci et al. (2010) found significant improvement in both systolic and diastolic blood

pressures with supervised aerobic and resistance training [28]. The inconsistencies among the studies may reflect the different interventions employed. Our meta-analysis found significant improvement with lifestyle intervention in the cardiovascular diseaseassociated risk factors BMI, HbA1c, SBP, and DBP (all Pvalues ≤ 0.014) in patients with type 2 diabetes. HDL-c and LDL-c levels were not significantly changed by lifestyle intervention (P = 0.503 and P = 0.092, respectively). Sensitivity analysis indicated that the HbA1c and BMI findings were

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343

Fig. 3 – Forest plot comparing intervention and control groups for change from baseline in (top to bottom) BMI, HbA1c, SBP, DBP, LDL-c and HDL-c. Abbreviations: CI, confidence interval; std diff, standardized difference. not dependent on any one study and did not result from publication bias. There are several strengths to our analysis. For example, we focused on long-term effects of lifestyle

interventions, since only studies that were > 6 months were included, and all included studies were randomized controlled trials.

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Fig. 4 – Sensitivity analysis of the influence of each study on the pooled estimate of (A) BMI or (B) HbA1c. The leave-one-out approach was used. Abbreviations: CI, confidence interval; std diff, standardized difference.

Our findings are consistent with several previous metaanalyses and systematic reviews which also found that multifaceted lifestyle intervention improved several cardiovascularassociated risk factors, including BMI and HbA1c, in patients with or at risk for type 2 diabetes [5–7,12,13]. One prior metaanalysis examined the effect of lifestyle intervention focused on physical activity (regular movement such as walking) and exercise (structured activities such as cycling, running etc.) on levels of HbA1c and BMI in patients with type 2 diabetes [5]. The meta-analysis included 17 randomized controlled trials and found that interventions which increased physical and exercise activity were associated with improvements in HbA1c (weighted mean difference [WMD], −0.32%, 95% CI, −0.44% to −0.21%) and BMI (WMD, −1.05 kg/m2, 95% CI, −1.31 to −0.80) [5]. Other meta-analyses and systematic reviews found that multi-faceted lifestyle intervention improved several cardiovascular-associated risk factors, including BMI and HbA1c, in

patients with or at risk for type 2 diabetes [6,7,10,12,13]. The lifestyle interventions included an exercise and diet component and at least one other component such as smoking cessation, behavior modification, and counseling. In contrast to our study, one of the meta-analysis did not find intervention significantly improves systolic or diastolic blood pressure [7]. It also found, using sensitivity analysis, that there was improvement in HDL (mean difference, 0.04; 95% CI, 0.03–0.05) and HbA1c (mean difference, −0.71; 95% CI, − 1.31 to 0–0.12) only for interventions that included pharmacotherapy [7]. In addition, these improvements did not continue past the interventional phase [7]. We did not evaluate the relationship of lifestyle intervention with pharmacotherapy or treatment duration in our analysis. Another meta-analysis specifically assessed whether resistance exercise is comparable to aerobic exercise in regard to glycemic control, blood lipids, blood pressure, anthropometric measures, health status, and adverse events [10]. Twelve

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Fig. 5 – Funnel plots for publication bias (A) BMI and (B) HbA1c. Abbreviations: std diff, standardized difference.

randomized controlled studies that included 626 patients with type 2 diabetes (≥ 18 years of age) were included in the metaanalysis. The analysis found that aerobic exercise was associated with a greater reduction in HbA1c compared with resistance exercise (18% difference [1.97 mmol/mol; 95% CI, 0.01–0.36]). However with sensitivity analysis, the difference was non-significant (P = 0.14). Significant differences from baseline in favor of aerobic exercise were also observed for BMI, peak oxygen consumption, and maximum heart rate. Importantly, the difference between exercise regimens was not clinically important, and the authors conclude that physical activity in general may be more important than the choice of a specific exercise [10]. One systematic review analyzed a combination of 3 groups of patients: those at risk for type 2 diabetes, those at risk for cardiovascular disease, and those with type 2 diabetes [6]. They found that lifestyle intervention did not improve SBP, DBP, or HDL. However, the fact their study evaluated a heterogeneous population of patients makes it difficult to compare their finding with ours. Similar to our findings, the analysis did not find lifestyle intervention affected LDL levels. Two other systematic reviews evaluated whether behavioral changes, such as exercise training/physical activity and/or nutritional intervention, impacted the incidence of type 2 diabetes in subjects at risk for the disease [12,13]. They found that although there was wide variability in efficacy, all the included studies indicated that behavioral changes that included modification of diet and exercise reduced the incidence of type 2 diabetes compared with controls, with a relative risk reduction of 39%–75%. The systematic review also found a benefit in weight change and a reduction in BMI. In

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addition, both reviews indicated that adopting a long-term approach in changing behavior with several interventional components was most successful. A literature review identified over 100 studies that assessed the role of physical activity on cardiovascular disease in subjects with diabetes [11]. The authors conclude that overall the literature suggests physical activity reduces the risk of cardiovascular disease in people with diabetes. However, they comment that a number of drug trials do not support the idea that reduction of blood glucose concentration reduces cardiovascular disease. Why exercise reduces the risk of cardiovascular disease in patients with diabetes is unclear. There are several limitations to our analysis that should be considered when interpreting the findings. The included studies used diverse forms of interventions and there was little detail regarding the specifics of intervention methodology. Due to the lack of experimental detail in many published studies, it is possible that other studies may have been missed due poor descriptions of lifestyle interventions. We grouped all the types of interventions for our analysis; hence, it is not possible to evaluate or compare the efficacy of each type of intervention with improving markers of cardiovascular disease. All included studies had a high risk for bias in regard to blinding of the participants and personnel that may have affected outcomes. The different included studies had a wide range of variability in age, sex, and duration of follow up which could have confounded our findings. Ideally, we would have used subgroup analysis to address this problem. However, due to the limitation of extracting sufficient data for each confounder, we were unable to perform this type of analysis. Another possible confounding factor is the potential difference between groups in drug prescriptions. Drug prescription information was only reported in 5 of the studies [21,23–25,31] and the data in these studies were not sufficient to allow us to perform multivariate analysis to adjust for differences in drug prescriptions. Although our funnel plot analysis indicated there was no publication bias, this conclusion is limited owing to the large degree of clinical heterogeneity across the included studies. We did not assess the effect of lifestyle intervention on death or adverse events due to cardiovascular disease; therefore, it is not clear how the changes we see in cardiovascular disease-associated risk factors reflect these clinical outcomes.

5.

Conclusion

In summary, our meta-analysis found that lifestyle intervention which included change in diet, exercise, and education showed significant benefit in a number of risk factors which are known to be associated with cardiovascular disease in patients with type 2 diabetes. Supplementary data to this article can be found online at http://dx.doi.org/10.1016/j.metabol.2014.10.018.

Author contributions Liang Chen: guarantor of integrity of the entire study; Jian-Hao Pei: study concepts; Jian Kuang: study design, statistical

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analysis; Hong-Mei Chen: data analysis; Zhong Chen: manuscript preparation; Zhong-Wen Li: manuscript editing; Hua-Zhang Yang: manuscript review.

Acknowledgments None.

Conflict of interest None.

REFERENCES

[1] Lloyd-Jones D, Adams R, Carnethon M, De Simone G, Ferguson TB, Flegal K, et al. Heart disease and stroke statistics–2009 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Circulation 2009;119:e21-181. [2] Deshpande AD, Harris-Hayes M, Schootman M. Epidemiology of diabetes and diabetes-related complications. Phys Ther 2008;88:1254–64. [3] Boule NG, Haddad E, Kenny GP, Wells GA, Sigal RJ. Effects of exercise on glycemic control and body mass in type 2 diabetes mellitus: a meta-analysis of controlled clinical trials. JAMA 2001;286:1218–27. [4] American Diabetes A. Standards of medical care in diabetes–2013. Diabetes Care 2013;36(Suppl. 1):S11–66. [5] Avery L, Flynn D, van Wersch A, Sniehotta FF, Trenell MI. Changing physical activity behavior in type 2 diabetes: a systematic review and meta-analysis of behavioral interventions. Diabetes Care 2012;35:2681–9. [6] Angermayr L, Melchart D, Linde K. Multifactorial lifestyle interventions in the primary and secondary prevention of cardiovascular disease and type 2 diabetes mellitus—a systematic review of randomized controlled trials. Ann Behav Med 2010;40:49–64. [7] Schellenberg ES, Dryden DM, Vandermeer B, Ha C, Korownyk C. Lifestyle interventions for patients with and at risk for type 2 diabetes: a systematic review and meta-analysis. Ann Intern Med 2013;159:543–51. [8] Yuen A, Sugeng Y, Weiland TJ, Jelinek GA. Lifestyle and medication interventions for the prevention or delay of type 2 diabetes mellitus in prediabetes: a systematic review of randomised controlled trials. Aust N Z J Public Health 2010;34: 172–8. [9] Brand T, Pischke CR, Steenbock B, Schoenbach J, Poettgen S, Samkange-Zeeb F, et al. What works in community-based interventions promoting physical activity and healthy eating? A review of reviews. Int J Environ Res Public Health 2014;11(6):5866–88. [10] Yang Z, Scott CA, Mao C, Tang J, Farmer AJ. Resistance exercise versus aerobic exercise for type 2 diabetes: a systematic review and meta-analysis. Sports Med 2014;44(4):487–99. [11] Koivula RW, Tornberg AB, Franks PW. Exercise and diabetes-related cardiovascular disease: systematic review of published evidence from observational studies and clinical trials. Curr Diab Rep 2013;13(3):372–80. [12] Norris SL, Zhang X, Avenell A, Gregg E, Schmid CH, Lau J. Long-term non-pharmacological weight loss interventions for adults with prediabetes. Cochrane Database Syst Rev 2005 (2):CD005270.

[13] Baker MK, Simpson K, Lloyd B, Bauman AE, Singh MA. Behavioral strategies in diabetes prevention programs: a systematic review of randomized controlled trials. Diabetes Res Clin Pract 2011;91(1):1–12. [14] Cochrane Handbook for Systematic Reviews of Interventions Version 5.1.0. [updated March 2011] , In: Higgens JPT, Green LA, editors. The Cochrane Collaboration; 2011. [15] Kadoglou NP, Iliadis F, Angelopoulou N, Perrea D, Ampatzidis G, Liapis CD, et al. The anti-inflammatory effects of exercise training in patients with type 2 diabetes mellitus. Eur J Cardiovasc Prev Rehabil 2007;14:837–43. [16] Look ARG, Wing RR. Long-term effects of a lifestyle intervention on weight and cardiovascular risk factors in individuals with type 2 diabetes mellitus: four-year results of the Look AHEAD trial. Arch Intern Med 2010;170:1566–75. [17] Coppell KJ, Kataoka M, Williams SM, Chisholm AW, Vorgers SM, Mann JI. Nutritional intervention in patients with type 2 diabetes who are hyperglycaemic despite optimised drug treatment–Lifestyle Over and Above Drugs in Diabetes (LOADD) study: randomised controlled trial. BMJ 2010;341:c3337. [18] Sone H, Tanaka S, Iimuro S, Tanaka S, Oida K, Yamasaki Y, et al. Long-term lifestyle intervention lowers the incidence of stroke in Japanese patients with type 2 diabetes: a nationwide multicentre randomised controlled trial (the Japan Diabetes Complications Study). Diabetologia 2010;53:419–28. [19] Trento M, Passera P, Bajardi M, Tomalino M, Grassi G, Borgo E, et al. Lifestyle intervention by group care prevents deterioration of Type II diabetes: a 4-year randomized controlled clinical trial. Diabetologia 2002;45:1231–9. [20] Ali M, Schifano F, Robinson P, Phillips G, Doherty L, Melnick P, et al. Impact of community pharmacy diabetes monitoring and education programme on diabetes management: a randomized controlled study. Diabet Med 2012;29:e326–33. [21] Crasto W, Jarvis J, Khunti K, Skinner TC, Gray LJ, Brela J, et al. Multifactorial intervention in individuals with type 2 diabetes and microalbuminuria: the Microalbuminuria Education and Medication Optimisation (MEMO) study. Diabetes Res Clin Pract 2011;93:328–36. [22] Salinero-Fort MA, Carrillo-de Santa Pau E, Arrieta-Blanco FJ, Abanades-Herranz JC, Martín-Madrazo C, Rodés-Soldevila B, et al. Effectiveness of PRECEDE model for health education on changes and level of control of HbA1c, blood pressure, lipids, and body mass index in patients with type 2 diabetes mellitus. BMC Public Health 2011;11:267. [23] Ko GT, Li JK, Kan EC, Lo MK. Effects of a structured health education programme by a diabetic education nurse on cardiovascular risk factors in Chinese Type 2 diabetic patients: a 1-year prospective randomized study. Diabet Med 2004;21:1274–9. [24] Uusitupa M, Laitinen J, Siitonen O, Vanninen E, Pyorala K. The maintenance of improved metabolic control after intensified diet therapy in recent type 2 diabetes. Diabetes Res Clin Pract 1993;19:227–38. [25] Wisse W, Boer Rookhuizen M, de Kruif MD, van Rossum J, Jordans I, ten Cate H, et al. Prescription of physical activity is not sufficient to change sedentary behavior and improve glycemic control in type 2 diabetes patients. Diabetes Res Clin Pract 2010;88:e10–3. [26] Krein SL, Klamerus ML, Vijan S, Lee JL, Fitzgerald JT, Pawlow A, et al. Case management for patients with poorly controlled diabetes: a randomized trial. Am J Med 2004;116:732–9. [27] Dobrosielski DA, Gibbs BB, Ouyang P, Bonekamp S, Clark JM, Wang NY, et al. Effect of exercise on blood pressure in type 2 diabetes: a randomized controlled trial. J Gen Intern Med 2012;27:1453–9. [28] Balducci S, Zanuso S, Nicolucci A, De Feo P, Cavallo S, Cardelli P, et al. Effect of an intensive exercise intervention strategy on modifiable cardiovascular risk factors in subjects with type 2

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diabetes mellitus: a randomized controlled trial: the Italian Diabetes and Exercise Study (IDES). Arch Intern Med 2010;170: 1794–803. [29] Kirk A, Mutrie N, MacIntyre P, Fisher M. Effects of a 12-month physical activity counselling intervention on glycaemic control and on the status of cardiovascular risk factors in people with Type 2 diabetes. Diabetologia 2004;47:821–32.

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[30] Sevick MA, Korytkowski M, Stone RA, Piraino B, Ren D, Sereika S, et al. Biophysiologic outcomes of the Enhancing Adherence in Type 2 Diabetes (ENHANCE) trial. J Acad Nutr Diet 2012;112: 1147–57. [31] Chan CW, Siu SC, Wong CK, Lee VW. A pharmacist care program: positive impact on cardiac risk in patients with type 2 diabetes. J Cardiovasc Pharmacol Ther 2012;17:57–64.